Design, synthesis, DNA-binding and cytotoxicity evaluation of new potential combilexines
C Hotzel, A Marotto, U Pindur
Index: Hotzel, Christian; Marotto, Annalisa; Pindur, Ulf European Journal of Medicinal Chemistry, 2002 , vol. 37, # 5 p. 367 - 378
Full Text: HTML
Citation Number: 16
Abstract
Combilexines, compounds in which a DNA intercalator is linked to a minor groove binding component, interact with the DNA in a sequence specific manner to yield in most cases compounds with anticancer activity. A series of new compounds closely related to netropsin in which the two components were linked by an amide group was synthesised as potential combilexines. As some of these compounds showed cytotoxic activity in vitro, an attempt ...
Related Articles:
Reactivity of a tetrahedral intermediate in hydrolysis of N??acetylpyrrole
[Journal of Heterocyclic Chemistry, , vol. 21, p. 975 - 976]
Reactivity of a tetrahedral intermediate in hydrolysis of N??acetylpyrrole
[Journal of Heterocyclic Chemistry, , vol. 21, p. 975 - 976]
Reactivity of a tetrahedral intermediate in hydrolysis of N??acetylpyrrole
[Journal of Heterocyclic Chemistry, , vol. 21, p. 975 - 976]
Total synthesis and stereochemical reassignment of the indole alkaloid vinoxine
[Tetrahedron Letters, , vol. 25, # 29 p. 3119 - 3122]